Melanoma types by in vivo reflectance confocal microscopy correlated with protein and molecular genetic alterations: A pilot study.
Adult
Aged
Aged, 80 and over
Biomarkers
/ metabolism
Cyclin D1
/ metabolism
Dermatology
Female
GTP Phosphohydrolases
/ genetics
Humans
Immunohistochemistry
In Situ Hybridization, Fluorescence
Male
Melanoma
/ diagnostic imaging
Membrane Proteins
/ genetics
Microscopy, Confocal
/ methods
Middle Aged
Mutation
Neoplasm Invasiveness
Pilot Projects
Proto-Oncogene Proteins B-raf
/ genetics
Proto-Oncogene Proteins c-kit
/ genetics
Retrospective Studies
Skin Neoplasms
/ diagnostic imaging
Melanoma, Cutaneous Malignant
Journal
Experimental dermatology
ISSN: 1600-0625
Titre abrégé: Exp Dermatol
Pays: Denmark
ID NLM: 9301549
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
received:
08
11
2018
revised:
21
12
2018
accepted:
07
01
2019
pubmed:
13
1
2019
medline:
30
7
2020
entrez:
13
1
2019
Statut:
ppublish
Résumé
Cutaneous melanoma (CM) is one of the most prevalent skin cancers, which lacks both a prognostic marker and a specific and lasting treatment, due to the complexity of the disease and heterogeneity of patients. Reflectance confocal microscopy (RCM) in vivo analysis is a versatile approach offering immediate morphological information, enabling the identification of four primary cutaneous RCM CM types. Whether RCM CM types are associated with a specific protein and molecular genetic profiles at the tissue level remains unclear. The current pilot study was designed to identify potential correlations between RCM CM types and specific biological characteristics, combining immunohistochemistry (IHC) and molecular analyses. Eighty primary CMs evaluated at patient bedside with RCM (type 1 [19, 24%], type 2 [12, 15%], type 3 [7, 9%] and type 4 [42, 52%]) were retrospectively evaluated by IHC stains (CD271, CD20, CD31, cyclin D1), fluorescence in situ hybridization FISH for MYC gain and CDKN2A loss and molecular analysis for somatic mutations (BRAF, NRAS and KIT). RCM CM types correlated with markers of stemness property, density of intra-tumoral lymphocytic B infiltrate and cyclin D1 expression, while no significant association was found with blood vessel density nor molecular findings. RCM CM types show a different marker profile expression, suggestive of a progression and an increase in aggressiveness, according to RCM morphologies.
Substances chimiques
Biomarkers
0
CCND1 protein, human
0
Membrane Proteins
0
Cyclin D1
136601-57-5
KIT protein, human
EC 2.7.10.1
Proto-Oncogene Proteins c-kit
EC 2.7.10.1
BRAF protein, human
EC 2.7.11.1
Proto-Oncogene Proteins B-raf
EC 2.7.11.1
GTP Phosphohydrolases
EC 3.6.1.-
NRAS protein, human
EC 3.6.1.-
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
254-260Subventions
Organisme : PRIN
ID : Prot-2012-JJX494
Pays : International
Informations de copyright
© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.